Gitelman syndrome (Q21202907)

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scientific article

Language	Label	Description	Also known as
English	Gitelman syndrome	scientific article

Statements

scholarly article

0 references

11 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

21 December 2019

29 May 2020

6 November 2020

19 November 2020

Gitelman syndrome (English)

0 references

Gitelman syndrome

11 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

21 December 2019

29 May 2020

6 November 2020

19 November 2020

genetic variation

1 reference

14 September 2019

transport protein

1 reference

28 November 2019

membrane proteins

1 reference

15 December 2019

1 reference

21 December 2019

1 reference

6 November 2020

1 reference

19 November 2020

Elena Levtchenko

2

author given names

Elena N

author last names

Levtchenko

object named as

Elena N Levtchenko

1 reference

Dimensions Publication ID

18 August 2022

author name string

Nine V A M Knoers

1

author given names

Nine VAM

author last names

Knoers

1 reference

Dimensions Publication ID

18 August 2022

language of work or name

0 references

publication date

30 July 2008

11 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

21 December 2019

29 May 2020

6 November 2020

19 November 2020

Orphanet Journal of Rare Diseases

11 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

14 September 2019

28 November 2019

15 December 2019

21 December 2019

29 May 2020

6 November 2020

19 November 2020

3

0 references

22

0 references

1

0 references

copyright license

Creative Commons Attribution 2.0 Generic

11 references

Europe PubMed Central

24 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

28 November 2019

Europe PubMed Central

15 December 2019

Europe PubMed Central

21 December 2019

Europe PubMed Central

29 May 2020

Europe PubMed Central

6 November 2020

Europe PubMed Central

19 November 2020

copyright status

0 references

on focus list of Wikimedia project

0 references

https://scigraph.springernature.com/pub.10.1186/1750-1172-3-22

0 references

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

19 March 2017

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

19 March 2017

Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

19 March 2017

Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

19 March 2017

A new familial disorder characterized by hypokalemia and hypomagnesemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

19 March 2017

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

12 September 2017

The structural unit of the thiazide-sensitive NaCl cotransporter is a homodimer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

12 September 2017

Dose related growth response to indometacin in Gitelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

12 September 2017

Effects of chemical chaperones on partially retarded NaCl cotransporter mutants associated with Gitelman's syndrome in a mouse cortical collecting duct cell line

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

27 September 2017

Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

29 November 2018

Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

29 November 2018

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518128

29 November 2018

Mutations in the Na-Cl cotransporter reduce blood pressure in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic renal failure, end-stage renal disease, and peritoneal dialysis in Gitelman's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gitelman's syndrome: towards genotype-phenotype correlations?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomagnesemia and chondrocalcinosis in Bartter's and Gitelman's syndrome: review of the pathogenetic mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/18667063

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1750-1172-3-22

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Dimensions Publication ID

0 references

Internet Archive ID

pubmed-PMC2518128

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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